ID

25751

Description

Study ID: 101468/169 Clinical Study ID: 101468/169 Study Title:A Phase III, Randomised, Double-blind, Placebo-controlled, Parallel Group Study of Six Months Treatment with Ropinirole CR as Adjunctive Therapy in Patients with Parkinson's Disease who are not Optimally Controlled on L-dopa Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00381472 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Parkinson Disease This is the Unscheduled form.

Keywords

Versions (1)
  1. 9/17/17 9/17/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 17, 2017

DOI

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License

Creative Commons BY-NC 3.0
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GSK Ropinirole in Patients Suffering from Parkinsons Disease Unscheduled 101468/169 NCT00381472

English

GSK Ropinirole in Patients Suffering from Parkinsons Disease Unscheduled 101468/169 NCT00381472

1 forms  
INVESTIGATIONAL PRODUCT
Description

INVESTIGATIONAL PRODUCT

Alias
UMLS CUI-1
C0304229
Blinded Dose Level
Description

Blinded Dose Level

Data type

integer

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0304229
Start Date
Description

Start Date

Data type

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
Stop Date
Description

Stop Date

Data type

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0304229
Investigational product Container Number
Description

Investigational product Container Number

Data type

integer

Alias
UMLS CUI [1,1]
C3898691
UMLS CUI [1,2]
C0449788
COMPLIANCE
Description

COMPLIANCE

Alias
UMLS CUI-1
C1321605
Total number of Tablets Dispensed
Description

Total number of Tablets Dispensed

Data type

integer

Alias
UMLS CUI [1,1]
C0805077
UMLS CUI [1,2]
C0039225
Total number of Tablets Returned
Description

Total number of Tablets Returned

Data type

integer

Alias
UMLS CUI [1,1]
C2699071
UMLS CUI [1,2]
C0039225
Has the subject missed investigational product for more than 3 consecutive days?
Description

Has the subject missed investigational product for more than 3 consecutive days?

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0304229
DISPENSING
Description

DISPENSING

Alias
UMLS CUI-1
C0947323
Dispense investigational product Record dispensing information in the Investigational Product and Compliance sections above.
Description

Dispense investigational product

Data type

boolean

Alias
UMLS CUI [1,1]
C0947323
UMLS CUI [1,2]
C0013230
General Information
Description

General Information

Alias
UMLS CUI-1
C1508263
Subject Number
Description

Subject Number

Data type

integer

Alias
UMLS CUI [1]
C2348585
Visit Date
Description

Visit Date

Data type

date

Alias
UMLS CUI [1]
C1320303
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Similar models

GSK Ropinirole in Patients Suffering from Parkinsons Disease Unscheduled 101468/169 NCT00381472

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
INVESTIGATIONAL PRODUCT
C0304229 (UMLS CUI-1)
Blinded Dose Level
Item
Blinded Dose Level
integer
C0178602 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Investigational product Container Number
Item
Investigational product Container Number
integer
C3898691 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Item Group
COMPLIANCE
C1321605 (UMLS CUI-1)
Total number of Tablets Dispensed
Item
Total number of Tablets Dispensed
integer
C0805077 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Total number of Tablets Returned
Item
Total number of Tablets Returned
integer
C2699071 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Has the subject missed investigational product for more than 3 consecutive days?
Item
Has the subject missed investigational product for more than 3 consecutive days?
boolean
C1321605 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Item Group
DISPENSING
C0947323 (UMLS CUI-1)
Dispense investigational product
Item
Dispense investigational product Record dispensing information in the Investigational Product and Compliance sections above.
boolean
C0947323 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
Item Group
General Information
C1508263 (UMLS CUI-1)
Subject Number
Item
Subject Number
integer
C2348585 (UMLS CUI [1])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
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